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Congenital Central Hypoventilation Syndrome

Published:2006-11-15 Issue:10 Volume:174 Page:1139-1144
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Berry-Kravis Elizabeth M.,Zhou Lili,Rand Casey M.,Weese-Mayer Debra E.

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference21 articles.

1. FAILURE OF AUTOMATIC CONTROL OF VENTILATION (ONDINEʼS CURSE)

2. Idiopathic Congenital Central Hypoventilation Syndrome

3. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

4. PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

5. Molecular analysis of congenital central hypoventilation syndrome

Cited by 206 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Central Hypoventilation Syndrome and Disorders of Control of Ventilation;Clinics in Chest Medicine;2024-09

2. A new nonsense pathogenic variant in exon 1 of PHOX2B leads to the diagnosis of congenital central hypoventilation syndrome with intra-familial variability;Archives de Pédiatrie;2024-09

3. Congenital central hypoventilation syndrome in korea: 20 years of clinical observation and evaluation of the ventilation strategy in a single center;European Journal of Pediatrics;2024-05-23

4. Knockdown of PHOX2B in the retrotrapezoid nucleus reduces the central CO2 chemoreflex in rats;eLife;2024-05-10

5. Knockdown of PHOX2B in the retrotrapezoid nucleus reduces the central CO2 chemoreflex in rats;eLife;2024-05-10

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